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HRID 11476作成日:2026年10月26日

Hexane → cis-1-[2-(1-Adamantyl)ethyl]-1-pentyl-3-[2-(4-pyridyl)cyclopropylmethyl]urea

https://huagongshe.com/reaction/11476

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物ChloroiodomethaneHCID 11644—
反応物Ammonium ChlorideHCID 25517—
反応物(Z)-1-[2-(1-adamantyl)ethyl]-1-pentyl-3-[3-(4-pyridyl)-2-propenyl]ureaHCID 10294976—
反応物HCID 178418750HCID 178418750—
溶媒1,2-DichloroethaneHCID 11—
溶媒Ethyl AcetateHCID 8857—
生成物cis-1-[2-(1-Adamantyl)ethyl]-1-pentyl-3-[2-(4-pyridyl)cyclopropylmethyl]ureaHCID 671187303.5%

反応手順

A 1.0 M solution of diethylzinc in hexane (3.1 ml, 3.1 mmol) and chloroiodomethane (0.44 ml, 6.1 mol) were added to a solution of (Z)-1-[2-(1-adamantyl)ethyl]-1-pentyl-3-[3-(4-pyridyl)-2-propenyl]urea (Compound No. 1-111) in anhydrous 1,2-dichloroethane (3 ml) under a nitrogen atmosphere and ice-cooling, and the mixture was stirred for one hour. A saturated aqueous ammonium chloride solution (10 ml) was added to the reaction mixture under ice-cooling, and the whole was stirred at room temperature for 20 minutes and distributed with ethyl acetate (20 ml) and a saturated aqueous ammonium chloride solution (10 ml). The organic layer was washed with a saturated aqueous sodium chloride solution (10 ml) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to give 9.0 mg (3.5%) of the titled compound as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098226B2
出典データセットuspto-grants-2006_08
ORD IDord-b777ff91edf849818303f364dcaebf2f
出典メモuspto-grants-2006_08